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鉴定能增加缺陷患者成纤维细胞细胞色素 c 氧化酶活性的药物候选物。

Identification of drug candidates which increase cytochrome c oxidase activity in deficient patient fibroblasts.

机构信息

Metabolism Research Programme, Research Institute, The Hospital for Sick Children, Toronto, ON, Canada.

出版信息

Mitochondrion. 2011 Mar;11(2):264-72. doi: 10.1016/j.mito.2010.10.002. Epub 2010 Nov 2.

Abstract

Cytochrome c oxidase (COX) activity reflects the expressed level of respiratory chain complexes, mtDNA levels, titer and mass of mitochondria. Activity is also indicative of the overall fitness of mt-transcription factors and the import, transcription and translation of mt-proteins. We have developed a high-throughput assay to measure COX activity using live cells to screen chemical libraries for compounds capable of increasing COX activity. These libraries have revealed four examples which elevated the activities of COX in NIH-3T3 fibroblasts and in fibroblasts from patients with COX defects independent of the peroxisome proliferator activated receptor family.

摘要

细胞色素 c 氧化酶(COX)活性反映了呼吸链复合物的表达水平、线粒体 DNA 水平、线粒体的浓度和质量。其活性还可以指示 mt 转录因子的整体功能以及 mt 蛋白的导入、转录和翻译。我们开发了一种高通量测定法,使用活细胞测量 COX 活性,以筛选能够增加 COX 活性的化合物文库。这些文库揭示了四个例子,它们可以独立于过氧化物酶体增殖物激活受体家族提高 NIH-3T3 成纤维细胞和 COX 缺陷患者成纤维细胞中的 COX 活性。

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